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DOXYCYCLINE HYCLATE - 0115-1208-08 - (DOXYCYCLINE HYCLATE)

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Drug Information of DOXYCYCLINE HYCLATE

Product NDC: 0115-1208
Proprietary Name: DOXYCYCLINE HYCLATE
Non Proprietary Name: DOXYCYCLINE HYCLATE
Active Ingredient(s): 75    mg/1 & nbsp;   DOXYCYCLINE HYCLATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of DOXYCYCLINE HYCLATE

Product NDC: 0115-1208
Labeler Name: Global Pharmaceuticals, Division of Impax Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090505
Marketing Category: ANDA
Start Marketing Date: 20110411

Package Information of DOXYCYCLINE HYCLATE

Package NDC: 0115-1208-08
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE (0115-1208-08)

NDC Information of DOXYCYCLINE HYCLATE

NDC Code 0115-1208-08
Proprietary Name DOXYCYCLINE HYCLATE
Package Description 30 TABLET, DELAYED RELEASE in 1 BOTTLE (0115-1208-08)
Product NDC 0115-1208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DOXYCYCLINE HYCLATE
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110411
Marketing Category Name ANDA
Labeler Name Global Pharmaceuticals, Division of Impax Laboratories Inc.
Substance Name DOXYCYCLINE HYCLATE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of DOXYCYCLINE HYCLATE


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